Nineteen established CRC risk variants identified by GWAS and their proxies considered in this study.
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aPosition based on dbSNP build 130.bMajor allele/minor allele among Europeans.cMinor allele frequencies from published reports.dLinkage disequilibrium between SNP and proxy in HapMap CEU.eNot on Affymetrix 6.0 array.fExcluded from analysis as proxy r2
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2015-12-02
